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ID

36355

Descrizione

Study ID: 109385 Clinical Study ID: 109385 Study Title: A Randomized, Open Label, 4 Period Crossover Study in Healthy Subjects to Determine the Effect of Particle Size on the Pharmacokinetics of a Single mg Dose of GW856553 Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00517543 Sponsor: GlaxoSmithKline Phase: Phase 1 Study Recruitment Status: Completed Generic Name: GW856553 Trade Name: N/A Study Indication: Chronic Obstructive Pulmonary Disease (COPD), Rheumatoid Arthritis, Atherosclerosis

Keywords

versioni (1)
  1. 06/05/19 06/05/19 -
Titolare del copyright

GlaxoSmithKline

Caricato su

6 maggio 2019

DOI

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Licenza

Creative Commons BY-NC 3.0
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    The Effect of Particle Size on the Pharmacokinetics of a Single mg Dose of GW856553 NCT00517543

    Inglese

    Pharmacogenetics - Pharmacogenetic Research Consent; Pharmacogenetics Research Withdrawal of Consent

    1 moduli  
    Pharmacogenetic Research Consent
    Descrizione

    Pharmacogenetic Research Consent

    Alias
    UMLS CUI-1
    C0021430
    UMLS CUI-2
    C2347500
    Has informed consent been obtained for PGx-Pharmacogenetic research?
    Descrizione

    Has informed consent been obtained for PGx-Pharmacogenetic research?

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1,1]
    C0021430
    UMLS CUI [1,2]
    C2347500
    If informed consent has been obtained, record date informed consent obtained.
    Descrizione

    If informed consent has been obtained, record date informed consent obtained.

    Tipo di dati

    date

    Alias
    UMLS CUI [1,1]
    C0021430
    UMLS CUI [1,2]
    C0011008
    If informed consent has been obtained, has a blood sample been collected for PGx-pharmacogenetic (DNA) research?
    Descrizione

    Has a blood sample been collected for PGx-pharmacogenetic (DNA) research?

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1,1]
    C2347500
    UMLS CUI [1,2]
    C0005834
    If a blood sample has been collected for PGx-pharmacogenetic (DNA) research, record date sample taken.
    Descrizione

    Date sample taken

    Tipo di dati

    date

    Alias
    UMLS CUI [1,1]
    C0031328
    UMLS CUI [1,2]
    C1302413
    If no informed consent has been obtained for PGx-Pharmacogenetic research, check reason.
    Descrizione

    If no informed consent has been obtained for PGx-Pharmacogenetic research, check reason.

    Tipo di dati

    text

    Alias
    UMLS CUI [1,1]
    C0031325
    UMLS CUI [1,2]
    C0021430
    UMLS CUI [1,3]
    C0392360
    If other reason for informed consent has not been obtained for PGx-Pharmacogenetic research, please specify.
    Descrizione

    Other reason for informed consent has not been obtained for PGx-Pharmacogenetic research

    Tipo di dati

    text

    Alias
    UMLS CUI [1,1]
    C0031325
    UMLS CUI [1,2]
    C0021430
    UMLS CUI [1,3]
    C0392360
    UMLS CUI [1,4]
    C0205394
    UMLS CUI [1,5]
    C2348235
    Withdrawal of consent for PGx (DNA) sample destruction
    Descrizione

    Withdrawal of consent for PGx (DNA) sample destruction

    Alias
    UMLS CUI-1
    C1707492
    UMLS CUI-2
    C1948029
    UMLS CUI-3
    C0178913
    Has subject withdrawn consent for PGx research?
    Descrizione

    Has subject withdrawn consent for PGx research?

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1,1]
    C1707492
    UMLS CUI [1,2]
    C0031325
    If subject has withdrawn consent for PGx research, record date informed consent withdrawn
    Descrizione

    If subject has withdrawn consent for PGx research, record date informed consent withdrawn

    Tipo di dati

    date

    Alias
    UMLS CUI [1,1]
    C1707492
    UMLS CUI [1,2]
    C0031325
    UMLS CUI [1,3]
    C0011008
    Has a request been made for sample destruction?
    Descrizione

    Has a request been made for sample destruction?

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1,1]
    C1948029
    UMLS CUI [1,2]
    C0178913
    UMLS CUI [1,3]
    C1272683
    If a request has been made for sample destruction check reason
    Descrizione

    If a request has been made for sample destruction check reason

    Tipo di dati

    text

    Alias
    UMLS CUI [1,1]
    C1948029
    UMLS CUI [1,2]
    C0178913
    UMLS CUI [1,3]
    C1272683
    UMLS CUI [1,4]
    C0392360
    If other reason for request has been made for sample destruction, please specify
    Descrizione

    If other reason for request has been made for sample destruction, please specify

    Tipo di dati

    text

    Alias
    UMLS CUI [1,1]
    C1948029
    UMLS CUI [1,2]
    C0178913
    UMLS CUI [1,3]
    C1272683
    UMLS CUI [1,4]
    C0392360
    UMLS CUI [1,5]
    C0392360
    UMLS CUI [1,6]
    C0205394
    UMLS CUI [1,7]
    C2348235
    Ritorna all'inizio della pagina

    Similar models

    Pharmacogenetics - Pharmacogenetic Research Consent; Pharmacogenetics Research Withdrawal of Consent

    1 moduli
    Name
    genere
    Description | Question | Decode (Coded Value)
    Tipo di dati
    Alias
    Item Group
    Pharmacogenetic Research Consent
    C0021430 (UMLS CUI-1)
    C2347500 (UMLS CUI-2)
    Has informed consent been obtained for PGx-Pharmacogenetic research?
    Item
    Has informed consent been obtained for PGx-Pharmacogenetic research?
    boolean
    C0021430 (UMLS CUI [1,1])
    C2347500 (UMLS CUI [1,2])
    If informed consent has been obtained, record date informed consent obtained.
    Item
    If informed consent has been obtained, record date informed consent obtained.
    date
    C0021430 (UMLS CUI [1,1])
    C0011008 (UMLS CUI [1,2])
    Has a blood sample been collected for PGx-pharmacogenetic (DNA) research?
    Item
    If informed consent has been obtained, has a blood sample been collected for PGx-pharmacogenetic (DNA) research?
    boolean
    C2347500 (UMLS CUI [1,1])
    C0005834 (UMLS CUI [1,2])
    Date sample taken
    Item
    If a blood sample has been collected for PGx-pharmacogenetic (DNA) research, record date sample taken.
    date
    C0031328 (UMLS CUI [1,1])
    C1302413 (UMLS CUI [1,2])
    Item
    If no informed consent has been obtained for PGx-Pharmacogenetic research, check reason.
    text
    C0031325 (UMLS CUI [1,1])
    C0021430 (UMLS CUI [1,2])
    C0392360 (UMLS CUI [1,3])
    If no informed consent has been obtained for PGx-Pharmacogenetic research, check reason.
    Code List
    If no informed consent has been obtained for PGx-Pharmacogenetic research, check reason.
    CL Item
    Subject declined (1)
    CL Item
    Subject not asked by Investigator (2)
    CL Item
    Other, specify (Z)
    Other reason for informed consent has not been obtained for PGx-Pharmacogenetic research
    Item
    If other reason for informed consent has not been obtained for PGx-Pharmacogenetic research, please specify.
    text
    C0031325 (UMLS CUI [1,1])
    C0021430 (UMLS CUI [1,2])
    C0392360 (UMLS CUI [1,3])
    C0205394 (UMLS CUI [1,4])
    C2348235 (UMLS CUI [1,5])
    Item Group
    Withdrawal of consent for PGx (DNA) sample destruction
    C1707492 (UMLS CUI-1)
    C1948029 (UMLS CUI-2)
    C0178913 (UMLS CUI-3)
    Has subject withdrawn consent for PGx research?
    Item
    Has subject withdrawn consent for PGx research?
    boolean
    C1707492 (UMLS CUI [1,1])
    C0031325 (UMLS CUI [1,2])
    If subject has withdrawn consent for PGx research, record date informed consent withdrawn
    Item
    If subject has withdrawn consent for PGx research, record date informed consent withdrawn
    date
    C1707492 (UMLS CUI [1,1])
    C0031325 (UMLS CUI [1,2])
    C0011008 (UMLS CUI [1,3])
    Has a request been made for sample destruction?
    Item
    Has a request been made for sample destruction?
    boolean
    C1948029 (UMLS CUI [1,1])
    C0178913 (UMLS CUI [1,2])
    C1272683 (UMLS CUI [1,3])
    Item
    If a request has been made for sample destruction check reason
    text
    C1948029 (UMLS CUI [1,1])
    C0178913 (UMLS CUI [1,2])
    C1272683 (UMLS CUI [1,3])
    C0392360 (UMLS CUI [1,4])
    If a request has been made for sample destruction check reason
    Code List
    If a request has been made for sample destruction check reason
    CL Item
    Subject withdrew consent for PGx (3)
    CL Item
    Screen failure (2)
    CL Item
    Other, specify (Z)
    If other reason for request has been made for sample destruction, please specify
    Item
    If other reason for request has been made for sample destruction, please specify
    text
    C1948029 (UMLS CUI [1,1])
    C0178913 (UMLS CUI [1,2])
    C1272683 (UMLS CUI [1,3])
    C0392360 (UMLS CUI [1,4])
    C0392360 (UMLS CUI [1,5])
    C0205394 (UMLS CUI [1,6])
    C2348235 (UMLS CUI [1,7])
    Ritorna all'inizio della pagina 

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